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Nuvasive, Inc.

United States·US-MF-000007421

Last updated September 17, 2026

Information

Country: United States
Address: 7475, Lusk Blvd, San Diego, United States
Website: https://www.globusmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1-858-909-1800
PRRC Contact: Daniel S. Paul
EUDAMED SRN: US-MF-000007421
FDA FEI Number: 3002980729
DUNS Number: 053950783

Catalogue (44291)

Page 12 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	5230284P2	FDA UDI	Class II	Active
ReLine	13056080A	FDA UDI	Class II	Active
CoRoent	6774115	FDA UDI	Class II	Active
ReLine	13550000	FDA UDI	Class II	Active
ReLine	13016050	FDA UDI	Class II	Active
ReLine	13031055	FDA UDI	Class II	Active
NuVasive	6910612	FDA UDI	Class II	Active
Xlif	6999205	FDA UDI	Class I	Active
VuePoint	7901536	FDA UDI	Class II	Active
CoRoent	6251208	FDA UDI	Class I	Active
Armada	8992509	FDA UDI	Class I	Active
Armada	8563121	FDA UDI	Class II	Active
VuePoint	8980144P	FDA UDI	Class II	Active
Acp	8789585	FDA UDI	Class II	Active
ReLine	3737024	FDA UDI	Class II	Active
Modulus Expandable	1931128P2	FDA UDI	Class II	Active
CoRoent	5254364	FDA UDI	Class II	Active
CoRoent	6941244	FDA UDI	Class II	Active
Archon	8880321	FDA UDI	Class II	Active
CoRoent	6921245P	FDA UDI	Class II	Active
ReLine	11060070	FDA UDI	Class II	Active
ReLine	11087025	FDA UDI	Class II	Active
Xlif	XLIFNAVSINS	FDA UDI	Class II	Active
ReLine	10260414	FDA UDI	Class II	Active
Brigade	6968440	FDA UDI	Class II	Active
CoRoent	5184285P2	FDA UDI	Class II	Active
ReLine	REL5070POLYIMP	FDA UDI	Class II	Active
CoRoent	5144320P2	FDA UDI	Class II	Active
SpheRx	SPX2SR	FDA UDI	Class II	Active
ReLine	12055095	FDA UDI	Class II	Active
ReLine	15205500	FDA UDI	Class II	Active
ReLine	3700011	FDA UDI	Class II	Active
ReLine	3724550	FDA UDI	Class II	Active
ReLine	13086545	FDA UDI	Class II	Active
ReLine	13089040	FDA UDI	Class II	Active
CoRoent	1618293	FDA UDI	Class II	Active
Brigade	6942032	FDA UDI	Class II	Active
ReLine	12250045	FDA UDI	Class II	Active
Armada	8385040	FDA UDI	Class II	Active
StruXure	1595215	FDA UDI	Class II	Active
CoRoent	1657336	FDA UDI	Class II	Active
ReLine	13026575	FDA UDI	Class II	Active
Mas Plif	7070110	FDA UDI	Class I	Active
Xlif	3224130	FDA UDI	Class I	Active
ReLine	11019560	FDA UDI	Class II	Active
CoRoent	5224342	FDA UDI	Class II	Active
Precept	ALPMASDEXG	FDA UDI	Class II	Active
CoRoent	6712220	FDA UDI	Class II	Active
ReLine	11250130	FDA UDI	Class II	Active
ReLine	10100509	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

AJW Technology Consulting GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (36)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Nov 10, 2022	Z-0738-2023	—	open, classified	Potential that insert will be unable to disengage from the vertebral body replacement device/implant
Jul 19, 2022	Z-1052-2023	—	open, classified	Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.
Jun 20, 2022	Z-1453-2022	—	open, classified	Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.
Jun 10, 2020	Z-2684-2020	—	terminated	The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.
Feb 13, 2020	Z-1898-2020	—	terminated	Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
Jan 5, 2009	Z-0369-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0361-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0351-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0370-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0375-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0348-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0354-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0377-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0355-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0374-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0378-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0352-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0372-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0363-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0350-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0364-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0367-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0359-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0366-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0373-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0362-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0349-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0360-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0353-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0365-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0376-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0371-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0357-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0358-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0368-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0356-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.